Canonical Allele Identifier: CA393104775
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927687G>A , CM000677.2:g.73927687G>A GRCh38
NC_000015.9:g.74220028G>A , CM000677.1:g.74220028G>A GRCh37
NC_000015.8:g.72007081G>A NCBI36
NG_011466.1:g.6240G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.904G>A (LOXL1) MANE Select ENSP00000261921.7:p.Gly302Ser
ENST00000261921.7:c.904G>A (LOXL1) ENSP00000261921.7:p.Gly302Ser
ENST00000566011.5:c.904G>A (LOXL1) ENSP00000457827.1:p.Gly302Ser
NM_005576.2:c.904G>A (LOXL1) NP_005567.2:p.Gly302Ser
NR_040066.1:n.100C>T (LOXL1-AS1)
NR_040067.1:n.100C>T (LOXL1-AS1)
NR_040068.1:n.184+378C>T (LOXL1-AS1)
NR_040069.1:n.184+378C>T (LOXL1-AS1)
NR_040070.1:n.184+90C>T (LOXL1-AS1)
XM_011521555.1:c.904G>A (LOXL1) XP_011519857.1:p.Gly302Ser
XR_931824.1:n.1237G>A (LOXL1)
NM_005576.3:c.904G>A (LOXL1) NP_005567.2:p.Gly302Ser
XM_011521555.2:c.904G>A (LOXL1) XP_011519857.1:p.Gly302Ser
XR_931824.2:n.1226G>A (LOXL1)
NM_005576.4:c.904G>A (LOXL1) MANE Select NP_005567.2:p.Gly302Ser